Canonical Allele Identifier: PA915982843
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Ser31Asn
CA163957
NM_001257387.2:c.92G>A